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FDA 510(k)

VALU-PLUS PAD

K-Number: K925336 · 1993-02-12

ApplicantValmed, Inc.
Decision Date1993-02-12
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VALU-PLUS PAD is the device name listed in this FDA 510(k) record. The listed applicant is Valmed, Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K925336. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALU-PLUS PAD?

VALU-PLUS PAD is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Valmed, Inc.. The 510(k) number is K925336.

When did VALU-PLUS PAD receive FDA 510(k) clearance?

VALU-PLUS PAD received FDA 510(k) clearance on 1993-02-12, under 510(k) number K925336.

Who is the listed applicant for VALU-PLUS PAD?

The FDA 510(k) record lists Valmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALU-PLUS PAD?

The FDA product code for VALU-PLUS PAD is KNN.

Related Devices (Code: KNN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K211919KISS Dynamic Back Support, KISS Dynamic Solid Drop SeatKinetic Innovative Seating System, LLCK942309DYNASTY U1-31 (GELL/CELL)Foley & LardnerK942311DYNASTY U1-33 AGMFoley & LardnerK942308DYNASTY GC 12400 (GELL/CELL)Foley & LardnerK942310DYNASTY GC 12550 (GELL/CELL)Foley & LardnerK942312ALDEN LINEAGE WHEELCHAIR CUSHIONLewis W. Ward

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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